The ink can be used as a phosphor to fabricate down-converting green and white light-emitting diodes (LEDs). Waterborne anticounterfeiting inks suitable for screen printing were prepared via formula tuning for the anticounterfeit purpose. The anticounterfeiting luminescent patterns can be screen printed on paper, cloth, and poly(ethylene terephthalate) (PET), with encryption and decryption of information being accurately and conveniently realized by switching UV irradiation.Incorporating artificial photosensitizers with microorganisms has recently been recognized as an effective way to convert light energy into chemical energy. However, the incorporated biosystem is usually constructed in an extracellular manner and is vulnerable to the external environment. Here, we develop an intracellular hybrid biosystem in a higher organism protozoa Tetrahymena pyriformis, in which the in vivo synthesized CdS nanoparticles trigger photoreduction of nitrobenzene into aniline under visible-light irradiation. Integrating a photosensitizer CdS into T. pyriformis enables the photosensitizer CdS, inherent nitroreductase, and the cytoplasmic reductive substance in T. pyriformis to synergistically engage in the photocatalysis process, generating a greatly enhanced aniline yield with a 40-fold increment. Moreover, building an intracellular hybrid biosystem in mutant T. pyriformis could even grant it new capability of reducing nitrobenzene into aniline under visible-light irradiation. Such an intracellular hybrid biosystem paves a new way to functionalize higher organisms and diversify light energy conversion.The design of active cathode catalysts, with abundant active sites and outstanding catalytic activity for CO2 electroreduction, is important to promote the development of solid oxide electrolysis cells (SOECs). Herein, A-site-deficient perovskite oxide (La0.2Sr0.8)0.9Ti0.5Mn0.4Cu0.1O3-δ (LSTMC) is synthesized and studied as a promising cathode for SOECs. Cu nanoparticles can be rapidly and uniformly in situ-exsolved under reducing conditions. The heterostructure formed by the exsoluted Cu and LSTMC provides abundant active sites for the catalytic conversion of CO2 to CO. Combined with the remarkable oxygen-ion transport capacity of the LSTMC substrate, the specially designed Cu@LSTMC cathode exhibits a dramatically improved electrochemical performance. Furthermore, first-principles calculations proposed a mechanism for the adsorption and activation of CO2 by the heterostructure. Electrochemically, the Cu@LSTMC presents a high current density of 2.82 A cm-2 at 1.8 V and 800 °C, which is about 2.5 times higher than that of LSTM (1.09A cm-2).In this work, a self-circulation oxygen-hydrogen peroxide-oxygen (O2-H2O2-O2) system with photogenerated electrons as fuel and highly active hemin monomers as operators was engineered for ultrasensitive cathode photoelectrochemical bioassay of microRNA-141 (miRNA-141) using a stacked sealed paper device. During the circulation, the photogenerated electrons from BiVO4/Cu2O photosensitive structures assembled on a reduced graphene oxide paper electrode first reduced the electron acceptors (dissolved O2) to H2O2, which was then catalytically decomposed by hemin monomers to generate O2 again. The regenerated O2 continued to be reduced, which made O2 and H2O2 stuck in the infinite loop of O2-H2O2-O2 accompanied by the fast consumption of photogenerated electrons, generating an amplified photocurrent signal. When a target existed, a duplex-specific nuclease-induced target recycling reaction with dual trigger DNA probes as the output was performed to initiate the assembly of bridge-like DNA nanostructures, which endowed the self-circulation system with dual destruction functions as follows. (i) Reduced fuel supply the assembled DNA bridges acting as a negatively charged barrier prevented the photogenerated electrons from participating in the O2 reduction to H2O2. (ii) Incapacitation of operators DNA bridging induced the dimerization of hemin monomers linked on the DNA hairpins to catalytically inactive hemin dimers, leading to the abortive regeneration of O2. These destruction functions resulted in the circulation interruption and a remarkably decreased photocurrent signal. Thus, the developed cathode photoelectrochemical biosensing platform achieved ultrasensitive miRNA-141 detection with a linear range of 0.25 fM to 1 nM and a detection limit of 83 aM, and it also exhibited high accuracy, selectivity, and practicability.Intermediate temperature solid oxide fuel cells (IT-SOFCs) have been extensively studied due to high efficiency, cleanliness, and fuel flexibility. To develop highly active and stable IT-SOFCs for the practical application, preparing an efficient cathode is necessary to address the challenges such as poor catalytic activity and CO2 poisoning. Herein, an efficient optimized strategy for designing a high-performance cathode is demonstrated. By motivating the phase transformation of BaFeO3-δ perovskites, achieved by doping Pr at the B site, remarkably enhanced electrochemical activity and CO2 resistance are thus achieved. The appropriate content of Pr substitution at Fe sites increases the oxygen vacancy concentration of the material, promotes the reaction on the oxygen electrode, and shows excellent electrochemical performance and efficient catalytic activity. The improved reaction kinetics of the BaFe0.95Pr0.05O3-δ (BFP05) cathode is also reflected by a lower electrochemical impedance value (0.061 Ω?cm2 at 750 °C) and activation energy, which is attributed to high surface oxygen exchange and chemical bulk diffusion. https://www.selleckchem.com/products/resiquimod.html The single cells with the BFP05 cathode achieve a peak power density of 798.7 mW?cm-2 at 750 °C and a stability over 50 h with no observed performance degradation in CO2-containing gas. In conclusion, these results represent a promising optimized strategy in developing electrode materials of IT-SOFCs.Hydrocarbon-fueled solid oxide fuel cells (SOFCs) that can operate in the intermediate temperature range of 500-700 °C represent an attractive SOFC device for combined heat and power applications in the industrial market. One of the ways to realize such a device relies upon exploiting an in situ steam reforming process in the anode catalyzed by an anti-carbon coking catalyst. Here, we report a new Ni and Ru bimetal-doped perovskite catalyst, Ba(Zr0.1Ce0.7Y0.1Yb0.1)0.9Ni0.05Ru0.05O3-δ (BZCYYbNRu), with enhanced catalytic hydrogen production activity on n-butane (C4H10), which can resist carbon coking over extended operation durations. Ru in the perovskite lattice inhibits Ni precipitation from perovskite, and the high water adsorption capacity of proton conducting perovskite improves the coking resistance of BZCYYbNRu. When BZCYYbNRu is used as a steam reforming catalyst layer on a Ni-YSZ-supported anode, the single fuel cell not only achieves a higher power density of 1113 mW cm-2 at 700 °C under a 10 mL min-1 C4H10 continuous feed stream at a steam to carbon (H2O/C) ratio of 0.